Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP458778.RAJD6Pq3izK6eD7E912uLIckB3zuoJ19O9sL0kaVXNPNs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP458778.RAJD6Pq3izK6eD7E912uLIckB3zuoJ19O9sL0kaVXNPNs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP458778.RAJD6Pq3izK6eD7E912uLIckB3zuoJ19O9sL0kaVXNPNs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP458778.RAJD6Pq3izK6eD7E912uLIckB3zuoJ19O9sL0kaVXNPNs130_provenance.
- befree-2016 importedOn "2016-02-19" NP458778.RAJD6Pq3izK6eD7E912uLIckB3zuoJ19O9sL0kaVXNPNs130_provenance.
- NP458778.RAJD6Pq3izK6eD7E912uLIckB3zuoJ19O9sL0kaVXNPNs130_assertion wasGeneratedBy ECO_0000203 NP458778.RAJD6Pq3izK6eD7E912uLIckB3zuoJ19O9sL0kaVXNPNs130_provenance.
- NP458778.RAJD6Pq3izK6eD7E912uLIckB3zuoJ19O9sL0kaVXNPNs130_assertion wasDerivedFrom befree-2016 NP458778.RAJD6Pq3izK6eD7E912uLIckB3zuoJ19O9sL0kaVXNPNs130_provenance.
- NP458778.RAJD6Pq3izK6eD7E912uLIckB3zuoJ19O9sL0kaVXNPNs130_assertion SIO_000772 15351017 NP458778.RAJD6Pq3izK6eD7E912uLIckB3zuoJ19O9sL0kaVXNPNs130_provenance.
- NP458778.RAJD6Pq3izK6eD7E912uLIckB3zuoJ19O9sL0kaVXNPNs130_assertion evidence source_evidence_literature NP458778.RAJD6Pq3izK6eD7E912uLIckB3zuoJ19O9sL0kaVXNPNs130_provenance.
- NP458778.RAJD6Pq3izK6eD7E912uLIckB3zuoJ19O9sL0kaVXNPNs130_assertion description "[In this group, protein-O-linked mannose-beta1,2-N-acetylglucosaminyltransferase and protein-O-mannosyltransferase 1 are considered to be responsible for muscle-eye-brain disease and Walker-Warburg syndrome, respectively, by glycosylation of alpha-dystroglycan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP458778.RAJD6Pq3izK6eD7E912uLIckB3zuoJ19O9sL0kaVXNPNs130_provenance.